Package 68788-8722-6

{"route": ["ORAL"], "spl_id": "abb81337-86aa-40de-852c-f42dafe5cc56", "openfda": {"nui": ["N0000175430"], "unii": ["N7U69T4SZR"], "rxcui": ["312078"], "spl_set_id": ["d349d5b7-5658-46d6-9bba-e6f6361cebb9"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8722-3)", "package_ndc": "68788-8722-3", "marketing_start_date": "20240809"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8722-6)", "package_ndc": "68788-8722-6", "marketing_start_date": "20240809"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-8722-9)", "package_ndc": "68788-8722-9", "marketing_start_date": "20240809"}], "brand_name": "Olanzapine", "product_id": "68788-8722_abb81337-86aa-40de-852c-f42dafe5cc56", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "68788-8722", "generic_name": "Olanzapine", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olanzapine", "active_ingredients": [{"name": "OLANZAPINE", "strength": "5 mg/1"}], "application_number": "ANDA076255", "marketing_category": "ANDA", "marketing_start_date": "20240809", "listing_expiration_date": "20261231"}